495-83-0 Usage
Uses
1. Used in Pharmaceutical Industry:
Tigloidine is used as an active pharmaceutical ingredient for its various medicinal properties. The expression is: tigloidine is used as an active pharmaceutical ingredient for its medicinal properties.
2. Used in Chemical Synthesis:
Tigloidine is used as a starting material for the synthesis of various compounds, such as dihydrotigloidine and dibromodihydrotigloidine. The expression is: tigloidine is used as a starting material for chemical synthesis to produce other compounds.
3. Used in Research and Development:
Tigloidine serves as a valuable compound for research purposes, particularly in the study of alkaloids, their properties, and potential applications. The expression is: tigloidine is used as a research compound for studying alkaloids and their properties.
4. Used in Analytical Chemistry:
Tigloidine can be employed in analytical chemistry for the identification and characterization of alkaloids, as well as for the development of new analytical methods. The expression is: tigloidine is used in analytical chemistry for the identification and characterization of alkaloids and the development of new methods.
5. Used in Quality Control:
Tigloidine can be utilized in the quality control of pharmaceutical products containing alkaloids, ensuring the presence of the desired compound and assessing the purity of the product. The expression is: tigloidine is used in quality control for assessing the presence and purity of alkaloids in pharmaceutical products.
References
Barger, Martin, Mitchel1.,J. Chern. Soc., 1820 (1937)
Check Digit Verification of cas no
The CAS Registry Mumber 495-83-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 495-83:
(5*4)+(4*9)+(3*5)+(2*8)+(1*3)=90
90 % 10 = 0
So 495-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H21NO2/c1-4-9(2)13(15)16-12-7-10-5-6-11(8-12)14(10)3/h4,10-12H,5-8H2,1-3H3/b9-4-/t10-,11-/m1/s1
495-83-0Relevant academic research and scientific papers
Specificities of the enzymes of N-alkyltropane biosynthesis in Brugmansia and Datura
Boswell, Henry D.,Draì?ger, Birgit,McLauchlan, W. Russell,Portsteffen, Andreas,Robins, David J.,Robins, Richard J.,Walton, Nicholas J.
, p. 871 - 878 (2007/10/03)
The enzymes N-methylputrescine oxidase (MPO), the tropine-forming tropinone reductase (TRI), the pseudotropine-forming tropinone reductase (TRII), the tropine:acyl-CoA transferase (TAT) and the pseudotropine:acyl-CoA transferase (PAT) extracted from transformed root cultures of Datura stramonium and a Brugmansia candida x aurea hybrid were tested for their ability to accept a range of alternative substrates. MPO activity was tested with N-alkylputrescines and N-alkylcadaverines as substrates. TRI and TRII reduction was tested against a series of N-alkylnortropinones, N- alkylnorpelletierines and structurally related ketones as substrates. TAT and PAT esterification tests used a series of N-substituted tropines, pseudotropines, pelletierinols and pseudopelletierinols as substrates to assess the formation of their respective acetyl and tigloyl esters. The results generally show that these enzymes will accept alien substrates to varying degrees. Such studies may shed some light on the overall topology of the active sites of the enzymes concerned.
